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   <dc:title>Biodiesel synthesis in a solvent-free system by recombinant Rhizopus oryzae Lipase : study of the catalytic reaction progress</dc:title>
   <dc:creator>Canet Morral, Albert</dc:creator>
   <dc:creator>Benaiges, M. Dolors</dc:creator>
   <dc:creator>Valero Barranco, Francisco</dc:creator>
   <dc:subject>Matèries del catàleg</dc:subject>
   <dc:subject>Immobilization</dc:subject>
   <dc:subject>Biodiesel</dc:subject>
   <dc:subject>Monoacylglycerols</dc:subject>
   <dc:subject>Recombinant Rhizopus oryzae lipase</dc:subject>
   <dc:subject>Response surface model</dc:subject>
   <dcterms:abstract>The recombinant 1,3-positional selective Rhizopus oryzae lipase (rROL) was used to synthesize biodiesel and monoacylglycerols simultaneously. The reaction was carried out in a solvent-free system with the enzyme immobilized on octadecyl-Sepabeads. Using response surface methodology, the methyl ester yield was optimized by means of the study of the effect of water, substrate molar ratio (methanol:olive oil) and methanol stepwise addition. It was concluded that in order to prevent enzyme inactivation by methanol, alcohol should be added slowly; otherwise a large amount of water would be present. Taking the best conditions, a 50.3 % yield was achieved in 3 h, which corresponds to 75.4 % of the acyl groups at the 1,3-position undergoing transesterification. It was also concluded that methyl esters result from the esterification of the free fatty acid hydrolyzed by the enzyme and also from a direct transesterification of oil. In addition, the fatty acid selectivity of rROL was found not to favor one fatty acid in olive oil over another.</dcterms:abstract>
   <dcterms:issued>2014</dcterms:issued>
   <dc:type>Article</dc:type>
   <dc:relation>Ministerio de Ciencia e Innovación CTQ2010-15131</dc:relation>
   <dc:relation>Generalitat de Catalunya 2009/SGR-281</dc:relation>
   <dc:relation>Generalitat de Catalunya 2010/CONE3-00063</dc:relation>
   <dc:relation>Journal of the American Oil Chemists' Society ; Vol. 91, Num. 9 (2014), p. 1499-1506</dc:relation>
   <dc:rights>open access</dc:rights>
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   <dc:rights>https://rightsstatements.org/vocab/InC/1.0/</dc:rights>
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